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FDA 510(k)

HAND HELD GONIOMETER

K-Number: K850082 · 1985-04-04

ApplicantChattanooga Group, Inc.
Decision Date1985-04-04
Product CodeKQW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HAND HELD GONIOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group, Inc.. It received FDA 510(k) clearance on 1985-04-04 under 510(k) number K850082. The device is classified under product code KQW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAND HELD GONIOMETER?

HAND HELD GONIOMETER is a medical device that received FDA 510(k) clearance on 1985-04-04. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K850082.

When did HAND HELD GONIOMETER receive FDA 510(k) clearance?

HAND HELD GONIOMETER received FDA 510(k) clearance on 1985-04-04, under 510(k) number K850082.

Who is the listed applicant for HAND HELD GONIOMETER?

The FDA 510(k) record lists Chattanooga Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAND HELD GONIOMETER?

The FDA product code for HAND HELD GONIOMETER is KQW.

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Other records listing Chattanooga Group, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: KQW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K926237O'BRIEN GONIOMETERSgarlato Laboratories, Inc.K901744DOBBHOFF(R) RETRIEVAL FORCEPSBiosearch Medical Products, Inc.K870767THE (CROM) TESTERTwin City Surgical, Inc.K831550FINGER BONIOMETER BK7506Fred Sammons, Inc.K812778THE TELOS EQUIPMENTThe Telos Co.K810441UNIVERSAL GONIMETERFred Sammons, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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